Canonical Allele Identifier: PA2830204541
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535557

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ser32936Thr
CA1985096
NM_133378.4:c.98807G>C